Hormonal and Reproductive Risk Factors for Sporadic Microsatellite Stable and Unstable Endometrial Tumors

被引:13
作者
Amankwah, Ernest K. [1 ]
Friedenreich, Christine M. [3 ,4 ,5 ]
Magliocco, Anthony M. [2 ]
Brant, Rollin [6 ]
Speidel, Thomas [3 ]
Rahman, Wahida [5 ]
Cook, Linda S. [3 ,4 ,7 ]
机构
[1] Univ S Florida, Coll Med, H Lee Moffitt Canc Ctr & Res Inst, Dept Canc Epidemiol, Tampa, FL 33612 USA
[2] Univ S Florida, Coll Med, H Lee Moffitt Canc Ctr & Res Inst, Dept Anat Pathol, Tampa, FL 33612 USA
[3] Alberta Hlth Serv, Calgary, AB, Canada
[4] Univ Calgary, Dept Oncol, Calgary, AB, Canada
[5] Univ Calgary, Dept Community Hlth Sci, Calgary, AB, Canada
[6] Univ British Columbia, Dept Stat, Vancouver, BC V5Z 1M9, Canada
[7] Univ New Mexico, Dept Internal Med, Albuquerque, NM 87131 USA
基金
加拿大健康研究院;
关键词
CANCER-RISK; POSTMENOPAUSAL WOMEN; COLORECTAL-CANCER; LYNCH-SYNDROME; INSTABILITY; CARCINOMA; THERAPY; HEALTH; CONTRACEPTION; ESTROGENS;
D O I
10.1158/1055-9965.EPI-13-0105
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hormonal and reproductive factors modulate bioavailable estrogen to influence endometrial cancer risk. Estrogen affects the microsatellite status of tumors, but the relation between these estrogen-related factors and microsatellite instability (MSI) status of endometrial tumors is not known. We evaluated associations between hormonal and reproductive factors and risks of microsatellite stable (MSS) and MSI endometrial cancer among postmenopausal women (MSS cases = 258, MSI cases = 103, and controls = 742) in a population-based case-control study in Alberta, Canada (2002-2006). Polytomous logistic regression was used to estimate ORs and 95% confidence intervals (95% CI). We observed a significant trend in risk reduction for MSI (P-trend = 0.005) but not MSS (P-trend = 0.23) cancer with oral contraceptive use; with 5-year use or more, the risk reduction was stronger for MSI (OR = 0.42; 95% CI, 0.23-0.77) than for MSS cancer (OR = 0.80; 95% CI, 0.54-1.17; P-heterogeneity = 0.05). For more recent use (<30 years), the risk reduction was stronger for MSI (OR = 0.36; 95% CI, 0.19-0.69) than for MSS cancer (OR = 0.77; 95% CI, 0.51-1.15; P-heterogeneity = 0.032). No differential risk associations were observed for menopausal hormone use, parity and age at menarche, menopause or first pregnancy. We found limited evidence for statistical heterogeneity of associations of endometrial cancer risk with hormonal and reproductive factors by MSI status, except with oral contraceptive use. This finding suggests a potential role for the MMR system in the reduction of endometrial cancer risk associated with oral contraceptive use, although the exact mechanism is unclear. This study shows for the first time that oral contraceptive use is associated with a reduced risk for MSI but not for MSS endometrial cancer. (C) 2013 AACR.
引用
收藏
页码:1325 / 1331
页数:7
相关论文
共 30 条
[1]   Menopausal Hormone Therapy and Risk of Endometrial Carcinoma Among Postmenopausal Women in the European Prospective Investigation into Cancer and Nutrition [J].
Allen, Naomi E. ;
Tsilidis, Konstantinos K. ;
Key, Timothy J. ;
Dossus, Laure ;
Kaaks, Rudolf ;
Lund, Eiliv ;
Bakken, Kjersti ;
Gavrilyuk, Oxana ;
Overvad, Kim ;
Tjonneland, Anne ;
Olsen, Anja ;
Fournier, Agnes ;
Fabre, Alban ;
Clavel-Chapelon, Francoise ;
Chabbert-Buffet, Nathalie ;
Sacerdote, Carlotta ;
Krogh, Vittorio ;
Bendinelli, Benedetta ;
Tumino, Rosario ;
Panico, Salvatore ;
Bergmann, Manuela ;
Schuetze, Madlen ;
van Duijnhoven, Fraenzel J. B. ;
Bueno-de-Mesquita, H. Bas ;
Onland-Moret, N. Charlotte ;
van Gils, Carla H. ;
Amiano, Pilar ;
Barricarte, Aurelio ;
Chirlaque, Maria-Dolores ;
Molina-Montes, Maria-Esther ;
Redondo, Maria-Luisa ;
Duell, Eric J. ;
Khaw, Kay-Tee ;
Wareham, Nick ;
Rinaldi, Sabina ;
Fedirko, Veronika ;
Mouw, Traci ;
Michaud, Dominique S. ;
Riboli, Elio .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2010, 172 (12) :1394-1403
[2]  
Amankwah EK, 2013, AM J EPIDEMIOL
[3]  
[Anonymous], 2012, CAN CANC STAT 2012
[4]  
Basil JB, 2000, CANCER-AM CANCER SOC, V89, P1758, DOI 10.1002/1097-0142(20001015)89:8<1758::AID-CNCR16>3.0.CO
[5]  
2-A
[6]  
Beral V, 2005, LANCET, V365, P1543, DOI 10.1016/S0140-6736(05)66455-0
[7]  
Boland CR, 1998, CANCER RES, V58, P5248
[8]   REPRODUCTIVE, MENSTRUAL, AND MEDICAL RISK-FACTORS FOR ENDOMETRIAL CANCER - RESULTS FROM A CASE-CONTROL STUDY [J].
BRINTON, LA ;
BERMAN, ML ;
MORTEL, R ;
TWIGGS, LB ;
BARRETT, RJ ;
WILBANKS, GD ;
LANNOM, L ;
HOOVER, RN .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1992, 167 (05) :1317-1325
[9]   Purposeful selection of variables in logistic regression [J].
Bursac, Zoran ;
Gauss, C. Heath ;
Williams, David Keith ;
Hosmer, David W. .
SOURCE CODE FOR BIOLOGY AND MEDICINE, 2008, 3 (01)
[10]   Oral contraceptives and reproductive system cancer [J].
Deligeoroglou, E ;
Michailidis, E ;
Creatsas, G .
WOMEN'S HEALTH AND DISEASE: GYNECOLOGIC AND REPRODUCTIVE ISSUES, 2003, 997 :199-208